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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2175879Generated: October 31, 2026

Dimethylformamide → 4-Bromo-2-fluoro-3-methoxybenzonitrile

https://huagongshe.com/reaction/2175879

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantCyanuric chlorideHCID 7954—
ReactantOxalyl chlorideHCID 65578—
Reactant4-Bromo-2-fluoro-3-methoxybenzoic acidHCID 16102676—
SolventDichloromethaneHCID 6344—
Product4-Bromo-2-fluoro-3-methoxybenzonitrileHCID 71270750—

Reaction Conditions

Temperature25 °C

Reaction Steps

Oxalyl chloride (20 mL) was added dropwise at 0° C. to a suspension of 4-bromo-2-fluoro-3-methoxybenzoic acid (8.30 g, 33.3 mmol) in 100 mL of DCM with 0.5 mL of DMF. The mixture was stirred at 25° C. for 2 hours and the clear solution was concentrated to dryness under reduced pressure. The residue dissolved in 60 mL of anhydrous acetonitrile was added to 600 mL of aqueous NH3.H2O at 0° C. and stirred for 2 hours then extracted with EtOAc twice. The combined EtOAc layer was washed with water and brine, dried over anhydrous Na2SO4 and concentrated. The residue (6.9 g) was dissolved in 60 mL of DMF and cooled to 0° C. with ice/water bath. Cyanuric chloride (7.70 g, 41.7 mmol) was added and stirred for 2 hours at 0° C. before poured to ice/water. The solid was collected by filtration and was washed with water, dissolved in DCM, dried over anhydrous Na2SO4 and concentrated to afford 4-bromo-2-fluoro-3-methoxybenzonitrile.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09062070B2
Source datasetuspto-grants-2015_06
ORD IDord-31d8e603b6524e94b14a7e37163392a6
Source noteuspto-grants-2015_06